Evidence map›Paper›PMID 35285130›Full record

ArticleJournal of cellular and molecular medicine2022

ANGPTL4 regulate glutamine metabolism and fatty acid oxidation in nonsmall cell lung cancer cells.

Song Xiao, Wang Nai-Dong, Yan Jin-Xiang, Tian Long, Lu Xiu-Rong, Gao Hong, Yan Jie-Cheng, Zhang Fei

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 47 citations in OpenAlex.

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  16. Journal of cardiovascular development and disease · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Song XiaoRadiotherapy Department, the First Affiliated Hospital of Hebei North University, Zhangjiakou, China.ORCID 0000-0002-4331-9535
Wang Nai-DongDepartment of Pharmacy, Ji Nan Hospital, Jinan, China.
Yan Jin-XiangNeurosurgery Department, Ningyang NO.1 People's Hospital, Ningyang, China.
Tian LongRadiotherapy Department, the First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Lu Xiu-RongRadiotherapy Department, the First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Gao HongRadiotherapy Department, Beijing Hospital, Beijing, China.
Yan Jie-ChengRadiotherapy Department, the First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Zhang FeiRadiotherapy Department, the First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Hebei North University · CNBeijing Hospital · CNJinan Infectious Disease Hospital · CNNingbo No.6 Hospital · CN

Funding

the Subject of ZHANGJIAKOU 1821155H
6 · The paper itself

Abstract

Angiopoietin-like protein (ANGPTL) 4 is a key factor in the regulation of lipid and glucose metabolism in metabolic diseases. ANGPTL4 is highly expressed in various cancers, but the regulation of energy metabolism in tumours remains to be determined. This study explored the role of ANGPTL4 in aerobic glycolysis, glutamine consumption and fatty acid oxidation in nonsmall cell lung cancer (NSCLC) cells. Two NSCLC cell lines (A549 and H1299) were used to investigate the role of ANGPTL4 in energy metabolism by tracer techniques and with Seahorse XF technology in ANGPTLs4 knockdown cells. RNA microarrays and specific inhibitors were used to identify targets in ANGPTLs4-overexpressing cells. The results showed that knockdown of ANGPTLs4 could inhibit energy metabolism and proliferation in NSCLC. ANGPTLs4 had no significant effect on glycolysis but affected glutamine consumption and fatty acid oxidation. Knockdown of ANGPTLs4 also significantly inhibited tumour metastasis and energy metabolism in mice and had a weak effect on glycolysis. RNA microarray analysis showed that ANGPTLs4 significantly affected glutaminase (GLS) and carnitine palmitoyl transferase 1 (CPT1). ANGPTLs4-overexpressing cells were exposed to a glutamine deprivation environment, and cell proliferation and energy metabolism were significantly decreased but still differed from normal NSCLC cells. Treatment of ANGPTLs4-overexpressing cells with GLS and CPT1 inhibitors simultaneously prevented the regulatory effects on cell proliferation and energy metabolism. ANGPTLs4 could promote glutamine consumption and fatty acid oxidation but not glycolysis or accelerate energy metabolism in NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsCell Line, TumorCell ProliferationFatty AcidsGlutamineGlycolysisMiceFatty AcidsGlutamineaerobic glycolysisANGPTL4fatty acid oxidationglutamineNSCLC

Identifiers

PMID35285130
PMCPMC8980907
OpenAlexW4220666763

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.